"Guise" all-titanium, all-artificial hearing ossicle replacement - Taiwan Registration b27ed569d832c8415fa63951a08cd8be
Access comprehensive regulatory information for "Guise" all-titanium, all-artificial hearing ossicle replacement in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b27ed569d832c8415fa63951a08cd8be and manufactured by GYRUS ENT LLC, A WHOLLY OWNED SUBSIDIARY OF GYRUS ACMI, INC.. The authorized representative in Taiwan is MEDFRONT MEDICAL TECHNOLOGY CORPORATION.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Product Details
For details, it is Chinese approved copy of the imitation order
G ENT Science
G.3495 Whole-hearing ossicle exchange
import
Dates and Status
May 02, 2007
May 02, 2017
Nov 20, 2019
Cancellation Information
Logged out
่จฑๅฏ่ญๅทฒ้พๆๆๆ